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BEUDAMED

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61 results · 48ms · Sources: EU EUDAMED, US FDA

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Country

China 18 Ireland 4 Israel 4 Türkiye 4 Australia 3 Bulgaria 2 Hungary 2 Japan 2 Thailand 2 Finland 1 Hong Kong 1 India 1 Poland 1 Singapore 1 South Korea 1 Taiwan 1 United States 1 + More Countries

Competent Authority

De/Ca304 Marktüberwachung Medizinprodukte Bayern 8 Ministry Of Health, Welfare And Sports 8 Malta Medicines Authority 7 Health Products Regulatory Authority, Medical Devices Department 5 Turkish Medicine And Medical Devices Agency 4 De/Ca05 Behorde Fur Justiz Und Verbraucherschutz 3 Federal Agency For Medicines And Health Products / / Health Products Division 3 Agencia Española De Medicamentos Y Productos Sanitarios 2 Bulgarian Drug Agency Department "Market Supervision And Lnspections" Division "Medical Devices" 2 De/Ca22 Bezirksregierung Münster 2 De/Ca70 Landesamt Für Umwelt Und Arbeitsschutz 2 Danish Medicines Agency, Pharmacovigilance & Medical Devices 2 Nemzeti Népegészségügyi és Gyógyszerészeti Központ 2 The Medicines And Healthcare Products Regulatory Agency 2 Agence Nationale De Sécurité Du Médicament Et Des Produits De Santé 1 Austrian National Public Health Institute 1 De/Ca09 Staatliches Gewerbeaufsichtsamt Hannover 1 De/Ca19 Bezirksregierung Detmold Dezernat 24 1 De/Ca20, Bezirksregierung Düsseldorf Dezernat 24 1 De/Ca24 Regierungspräsidium Darmstadt Abteilung Arbeitsschutz Und Umwelt 1 + More Competent Authorities

Plasti-med Plastik Medikal Ürünler San. ve Tic. Ltd. Şti.

System producer

🇹🇷 Türkiye

Data last updated 04 / 2026. Visit the official EUDAMED website for up-to-date data.

BEUDAMED

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BEUDAMED

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EU MDR

EU MDR Medical Devices EU MDR Active Medical Devices EU MDR Class I Medical Devices EU MDR Class I Software Devices EU MDR Class IIa Medical Devices EU MDR Class IIa Software Devices EU MDR Class IIb Medical Devices EU MDR Class IIb Software Devices EU MDR Class III Medical Devices EU MDR Class III Software Devices EU MDR Implantable Medical Devices EU MDR Measuring Function Medical Devices EU MDR Software Medical Devices

EU IVDR

EU IVDR In Vitro Diagnostic Devices EU IVDR Class A In Vitro Diagnostic Devices EU IVDR Class A Software Devices EU IVDR Class B In Vitro Diagnostic Devices EU IVDR Class B Software Devices EU IVDR Class C In Vitro Diagnostic Devices EU IVDR Class C Software Devices EU IVDR Class D In Vitro Diagnostic Devices EU IVDR Class D Software Devices EU IVDR Instrument Devices EU IVDR Kit Devices EU IVDR Reagent Devices EU IVDR Software Devices

FDA

FDA Medical Devices FDA Class I Medical Devices FDA Class II Medical Devices FDA Class III Medical Devices

By Country

EU IVDR Medical Devices from China EU IVDR Medical Devices from France EU IVDR Medical Devices from Germany EU IVDR Medical Devices from Romania EU IVDR Medical Devices from United States EU MDR Medical Devices from China EU MDR Medical Devices from Egypt EU MDR Medical Devices from Finland EU MDR Medical Devices from France EU MDR Medical Devices from Germany EU MDR Medical Devices from Italy EU MDR Medical Devices from Pakistan EU MDR Medical Devices from Poland EU MDR Medical Devices from Spain EU MDR Medical Devices from Türkiye EU MDR Medical Devices from United Kingdom EU MDR Medical Devices from United States

Notified Bodies

BSI Group The Netherlands B.V. DEKRA Certification B.V. DNV Product Assurance AS POLSKIE CENTRUM BADAN I CERTYFIKACJI S.A. SGS Belgium NV TÜV Rheinland LGA Products GmbH TÜV SÜD Product Service GmbH UDEM Uluslararasi Belgelendirme Denetim Egitim Merkezi San. ve Tic. A.Ş.

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